Assessment of Treatment Approaches and Outcomes in Stevens-Johnson Syndrome and Toxic Epidermal Necrolysis:Insights from a Pan-European Multicenter Study

Autor: Lars E. French, Brigitte Milpied, Viktorija Karpaviciute, Anna Oschmann, Annamari Ranki, Nicolas de Prost, Tine Lorentzen, Eva Oppel, Vesta Kucinskiene, Sapna Divani-Patel, Julie Loft Nagel, Saskia Ingen-Housz-Oro, Marie-Charlotte Brüggen, Mirjam Nägeli, Ser-Ling Chua, George-Sorin Tiplica, Khalaf Kridin, Artem Vorobyev, Eva Brezinova, Sarah Walsh, Florence Tetart, Skaidra Valiukeviciene, Carmen Salavastru, Biagio Didona, Anette Bygum

Publikováno v: Kridin, K, Brüggen, M C, Chua, S L, Bygum, A, Walsh, S, Nägeli, M C, Kucinskiene, V, French, L, Tétart, F, Didona, B, Milpied, B, Ranki, A, Salavastru, C, Březinová, E, Divani-Patel, S, Lorentzen, T, Nagel, J L, Valiukeviciene, S, Karpavičiūtė, V, Tiplica, G S, Oppel, E, Oschmann, A, De Prost, N, Vorobyev, A & Ingen-Housz-Oro, S 2021, ' Assessment of Treatment Approaches and Outcomes in Stevens-Johnson Syndrome and Toxic Epidermal Necrolysis : Insights from a Pan-European Multicenter Study ', JAMA Dermatology, vol. 157, no. 10, pp. 1182-1190 . https://doi.org/10.1001/jamadermatol.2021.3154
JAMA Dermatol

Importance: Stevens-Johnson syndrome (SJS) and toxic epidermal necrolysis (TEN) are severe drug reactions associated with a high rate of mortality and morbidity. There is no consensus on the treatment strategy. Objective: To explore treatment approac

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::013170af13795bf15fa5e0d47a6ffed5
https://portal.findresearcher.sdu.dk/da/publications/6dac307c-b894-40c2-b488-0139918beb6b

Spontaneous pneumothorax as a clinical manifestation of neurofibromatosis type 1

Autor: Tine Lorentzen, Anette Bygum, Hanne Madsen, Marie Josée Zareh Lausten-Thomsen

Publikováno v: Lorentzen, T, Madsen, H, Lausten-Thomsen, M J Z & Bygum, A 2021, ' Spontaneous pneumothorax as a clinical manifestation of neurofibromatosis type 1 ', BMJ Case Reports, vol. 14, no. 3, e238694 . https://doi.org/10.1136/bcr-2020-238694
BMJ Case Reports

Neurofibromatosis type 1 (NF1) is a genetic disorder affecting the skin, nervous system, eyes and bones. Pulmonary involvement is unknown to many physicians. Yet, patients may be affected by lung bullae and cysts, which represent an increased risk fo

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8acda9524e0f4e9f9f092dc25d0e62e3
https://findresearcher.sdu.dk:8443/ws/files/181296213/Open_Access_Version.pdf